RIO Execution Hub Sr. Associate
Pfizer · Mexico City, Mexico
RegulatoryFull-timeCompany career page
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Role summary
Senior Associate role managing multi-regional regulatory dossiers for assigned products and therapeutic areas. Responsible for end-to-end lifecycle management from initial registration through product withdrawal, quality assurance, and coordination with regional submission hubs to ensure timely and compliant delivery.
What they're looking for
- Bachelor's degree in Pharmacy, Life Sciences, Business, or Information Technology; or equivalent professional experience
- Advanced to fluent English proficiency; multilingual skills desirable
- Technical aptitude with demonstrated ability to learn new software, regulations, and quality standards
- Advanced Microsoft Office Suite skills
- Preferred: regulatory, quality, or compliance experience in pharmaceutical industry
- Preferred: familiarity with pharmaceutical organizational structures and country/cluster regulatory requirements
What you'll be doing
- Manage end-to-end regulatory dossiers for multi-regional submissions including initial applications and lifecycle management
- Perform quality review and approval of dossier components and table of contents for assigned submissions
- Author and review local regulatory documents such as cover letters, variations, and marketing authorization applications
- Partner with submission managers and hubs to deliver applications and meet prioritization timelines
- Identify, escalate, and support resolution of quality, compliance, and emerging risk issues
Privacy & handoff
This role links to Pfizer's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.